交配和温度对小地老虎雌蛾性信息素产生的影响

研究了交配和温度对小地老虎雌蛾性信息素产生的影响,结果表明,交配对性信息素各组分的滴度无显著影响,因此不影响小地老虎在下一暗期的再次求偶和交配.但环境温度对小地老虎性信息素的含量则有显著的影响,20～25℃最有利于小地老虎性信息素的生物合成,而低温和高温则均不利于小地老虎性信息素的正常产生与释放.     

杠柳新苷P和E对东方粘虫和小地老虎幼虫中肠蛋白酶活性的影响

从杀虫植物杠柳Periploca sepium Bunge根皮中分离得到的杠柳新苷P具有很高的杀虫活性, 为了探索其杀虫机理, 采用经典的昆虫蛋白酶活性测定方法, 比较研究了杠柳新苷P和无杀虫活性的杠柳新苷E对东方粘虫Mythimna separata与小地老虎Agrotis ypsilon 6龄幼虫中肠类胰蛋白酶和类胰凝乳蛋白酶活性的影响。结果表明： 对东方粘虫弱碱性类胰蛋白酶, 杠柳新苷P表现出强激活作用（酶活性为对照的3.43倍）, 激活时间可长达8 h, 而杠柳新苷E则无明显激活作用。杠柳新苷P和E对东方粘虫弱碱性类胰蛋白酶活性的影响二者差异显著（P=0.01）, 杠柳新苷P药后2, 4和8 h, 东方粘虫中肠弱碱性类胰蛋白酶的活性分别是杠柳新苷E药后的15.4, 106.8和242.7倍。酶活性测定结果还表明, 与东方粘虫相比, 小地老虎中肠类胰蛋白酶活性相对较低, 且杠柳新苷P的激活作用也较弱, 这可能是杠柳新苷P对东方粘虫具杀虫活性, 而小地老虎对其不敏感的原因之一; 另外, 杠柳新苷P和E对试虫中肠类凝乳胰蛋白酶活性均无明显影响。据此推测, 杠柳活性成分新苷P对东方粘虫中肠弱碱性类胰蛋白酶的激活作用可能是造成试虫中毒的机理之一。     

小地老虎及粘虫幼虫对灭幼脲表现自然耐药力的体壁结构和生化基础

小地老虎Agrotis ypsilon rottem.幼虫对灭幼脲具有一定的自然耐药力。本文以粘虫Mythimna separata(Walker)作为敏感性虫种与之进行比较,实验结果表明,灭幼脲对两种试虫的室内毒力相差4倍左右,引起差异的原因,在体壁结构方面主要在于:(1)小地老虎幼虫的表皮层较粘虫的厚4.2倍左右;(2)上表皮不是匀质结构,依靠少数蜡道与体表沟通;(3)几丁质片层内的孔道数较少,仅及粘虫的1/4。由此构成了表皮对疏水性的灭幼脲表现抗穿透的性能。小地老虎幼虫体壁还含有较强的生化防卫体系,灭幼脲对多功能氧化酶、芳基酰胺酶有明显激活效应,这两种酶都是灭幼脲的降解酶。由此认为,小地老虎幼虫对灭幼脲所表现的自然耐药力,是由体壁的抗穿透性能以及由灭幼脲所激活的适应酶所造成。     

Effects of periplocosides P and E from Periploca sepium on the proteinase activities in the midgut of larvae of Mythimna separata and Agrotis ypsilon ( Lepidoptera: Noctuidae)

从杀虫植物杠柳Periploca sepiutm Bunge根皮中分离得到的杠柳新苷P具有很高的杀虫活性,为了探索其杀虫机理,采用经典的昆虫蛋白酶活性测定方法,比较研究了杠柳新苷P和无杀虫活性的杠柳新苷E对东方粘虫Mythimna separata与小地老虎Agrotis ypsilon 6龄幼虫中肠类胰蛋白酶和类胰凝乳蛋白酶活性的影响.结果表明:对东方粘虫弱碱性类胰蛋白酶,杠柳新苷P表现出强激活作用(酶活性为对照的3.43倍),激活时间可长达8h,而杠柳新苷E则无明显激活作用.杠柳新苷P和E对东方粘虫弱碱性类胰蛋白酶活性的影响二者差异显著(P=0.01),杠柳新苷P药后2,4和8h,东方粘虫中肠弱碱性类胰蛋白酶的活性分别是杠柳新苷E药后的15.4,106.8和242.7倍.酶活性测定结果还表明,与东方粘虫相比,小地老虎中肠类胰蛋白酶活性相对较低,且杠柳新苷P的激活作用也较弱,这可能是杠柳新苷P对东方粘虫具杀虫活性,而小地老虎对其不敏感的原因之一;另外,杠柳新苷P和E对试虫中肠类凝乳胰蛋白酶活性均无明显影响.据此推测,杠柳活性成分新苷P对东方粘虫中肠弱碱性类胰蛋白酶的激活作用可能是造成试虫中毒的机理之一.     

劳氏粘虫发育起点温度和有效积温研究

【目的】明确劳氏粘虫Leucania loreyi (Duponchel)各虫态的发育起点温度和有效积温。【方法】本研究在光照培养箱中,测定劳氏粘虫分别在18、21、24、27、30℃下各虫态的发育历期,并运用有效积温法则计算出劳氏粘虫各虫态的发育起点温度和有效积温;采用Logisitic模型建立各虫态发育速率与温度的关系,进而求出各虫态的发育最适温度及适宜温区。【结果】劳氏粘虫各龄幼虫在18-30℃之间均能正常生长发育,发育历期随温度的升高而缩短。卵、幼虫、蛹、产卵前期和全世代的发育起点温度分别为11.83、13.89、14.20、﹣1.86和12.24℃,有效积温分别为52.55、254.53、118.15、121.89和542.26日·度。全世代的发育最适温度为20.71℃,发育适温区为12.65-28.78℃。【结论】根据广西代表地区气象资料,推算出劳氏粘虫在广西一年理论发生5.8-7.8代,与田间调查情况相符。     

日本沼虾精子的形态和超微结构研究

应用电子显微镜技术结合细胞化学方法对日本沼虾精子进行子形态和超微结构研究。结果显示,日本沼虾精子琪似外翻的伞状,无鞭毛,不运动的精子主要由前端棘突,中间帽状体和后主体部分组成,精子的核属非浓缩型,内布许多絮状物质,外无核膜包被,呈Ｆｅｕｌｇｅｎ阳性反应,位于后主体部内;中间帽状体的细胞质内含有一对中心粒和１５－２０根放射状排列的纤丝,纤丝在帽状体凸面中央汇聚并延伸成精子的棘突,棘突和放射状纤丝皆具     

鱼类精子活力研究进展

鱼类精子在精巢和精浆中一般不活动,只有当精子被排到体外并被外界环境的溶液稀释后才能活动．鱼类精子活力受渗透压、离子、ｐＨ 值、温度及ＣＯ２ 等因子的调节和影响, 不同的鱼类其精子活力有不同的调节方式;外界因子对鱼类精子活力的影响, 是通过影响ｃＡＭＰ－ＡＴＰ－Ｍｇ２＋ 系统来影响鞭毛的活动而实现的． 精子活力的评价指标主要有：精子激活后的运动时间、精子激活比例、精子运动速度及精子鞭毛摆动频率等． 大多数鱼类的精子,其活动能力是在生殖管道中获得的．     

褶纹冠蚌精子球的形态和超微结构观察

利用光镜和电镜技术研究了褶纹冠蚌精子球的形态和超微结构.结果表明:精子球呈球形,直径约65-70μm,容纳2300多个精子.从外向内,精子球由非细胞层、表面层和内部区组成.非细胞层薄,厚约0.6μm,易碎.表面层厚约7.5μm,被分隔成许多辐射状排列的小室,单个精子头部位于小室内,指向精子球的中央,而精子的单个鞭毛由精子球的表面伸出.精子质膜在鞭毛领处与表面层相连,相邻精子间无细胞质桥相连.内部区呈球状,内含絮状物质.精子球从雄蚌出水管排出后,位于精子球外周的鞭毛沿固定方向不停地摆动,精子球翻滚着向前运动,且单个精子依次从精子球上脱落下来,最后精子球成为一中空的球,历时120h.       

纹藤壶精子发生和成熟精子的超微结构

甲壳动物的精子形态各异.其中3个亚纲的精子具鞭毛,能运动,其它5个亚纲的精子无鞭毛且不运动.     

用麻饼发酵液诱杀粘虫和地老虎成虫

防治粘虫、地老虎的最有利时期是在成虫发生阶段,方法是以糖蜜诱杀剂诱杀为主,但是使用糖蜜诱杀剂在大面积上应用成本太高,因此我所进行了代用剂的研究。经过较长时间试验,结果证明以“麻饼发酵液”代替“糖蜜诱杀剂”效果良好。而且诱杀作用大于糖蜜诱杀剂,制法简单,成本低廉,宜于大面积应用。 一、试验结果 在1959年7月3～7日用两种液剂进行对比,其诱杀粘虫、地老虎成虫的效果如下表:     

THE EUPYRENE-APYRENE DICHOTOMOUS SPERMATOGENESIS OF LEPIDOPTERA. ORGAN CULTURE STUDY ON THE TIMING OF APYRENE COMMITMENT IN THE CODLING MOTH

Lepidopteran spermatogenesis is dichotomous, producing eupyrene (nucleated) and apyrene (anucleated) spermatozoa. The eupyrene precedes the apyrene spermatogenesis. The timing of the switchover from eupyrene to apyrene spermatogenesis was determined by cultivating testes of accurately aged codling moth larvae in a medium containing mammalian serum but neither hemolymph nor insect hormones. In cultures, eupyrene spermatogenesis occurred in testes dissected from either 4th or 5th instar larvae, probably due to macromolecular factor-like activity of the serum of the medium. But apyrene spermatogenesis occurred only in testes explanted during or after the fourth day of the 5th instar larva. It is concluded that: (1) An apyrene spermatogenesis inducing factor (ASIF) becomes active on the fourth day of the 5th instar larva in addition to the already existing macromolecular factor. (2) Primary spermatocytes can develop into either eupyrene or apyrene spermatozoa. (3) The apyrene spermatogenesis commitment and pupal commitment of other tissues coincide about the fourth day of the 5th instar larva.     

Inhibition of Spermiogenesis of Eupyrene Spermatozoa by Elevated,Sublethal Temperatures During Pupal-Adult Development of the Bertha Armyworm,Mamestra con figurata Wlk. (Lepidoptera,Noctuidae)

Summary

Eupyrene spermiogenesis and spermatozoa production in Mamestra configurata Walker were inhibited by temperatures >24° C during a “critical period” of about 7 days during the first half of post-diapause pupal-adult development. The critical period coincided with the appearance of early-stage eupyrene spermatids. If temperatures >24° C occurred during the critical period, eupyrene spermatozoa production was reduced, the result of irreversible autolysis of the early- and mid-stage eupyrene spermatids. Each day of exposure to 25 or 27.5° C during the critical period reduced the number of eupyrene cysts with spermatozoa on average by 12 to 14%. There were no observable effects on eupyrene spermiogenesis and spermatozoa production of exposing post-diapausing pupae to 25 or 27.5° C before or after the critical period. Apyrene spermatogenesis was not affected by 25 or 27.5° C.

Exposure of pupae to 25°or 27.5° C during diapause had no apparent effect on eupyrene spermiogenesis and spermatozoa production. Meiosis usually was not detected among the eupyrene cysts with lalje primary spermatocytes until after diapause, indicating that meiosis is suppressed during diapause. By providing a meiotic block, diapause governs the time of onset of the temperature-sensitive critical period of spermiogenesis. In nature, male pupae of M. configurata in diapause are protected from sterilizing temperatures in the soil during August and post-diapause developing pupae pass through the critical period of spermiogenesis in spring (April to June) when soil temperatures throughout the range of M. configurata in Canada are well below 25° C. The distribution of M. configurata in the northern region of the temperate zone may in part be attributable to the sensitivity of spermatogenesis to relatively mild temperatures.     

Precocious reprogramming of eupyrene-apyrene spermatogenesis commitment induced by allatectomy of the penultimate larval instar of the moth Actias selene

A possible causal relationship between the switch-over from eupyrene to apyrene spermatogenesis and pupation in Lepidoptera was examined in Actias selene. Precocious pupation, 11 days earlier than in the controls, was induced by allatectomy on the first day of the penultimate larval instar. The course of the eupyrene spermatogenesis, until nuclear elongation in the spermatid, is not related to pupation. In both allatectomized and control individuals, eupyrene metaphases appear 8 days after ecdysis of the fourth larval instar. Nuclear elongation, however, is triggered in the allatectomized individuals earlier than in the controls, probably by the premature decline of the juvenile hormone titre following allatectomy. Apyrene commitment, on the other hand, is directly related to pupation, as apyrene spermatogenesis begins 2 days after pupation in both control and allatectomized individuals.     

Behaviors of nucleus, basal bodies and microtubules during eupyrene and apyrene spermiogenesis in the silkworm, Bombyx mori (Lepidoptera)

Observations with immunostaining for tubulin and electron microscopy revealed that silkworm eupyrene spermiogenesis was characterized by an attachment of the basal body to the nucleus except in the period of movement for unidirectional arrangement. In young eupyrene sperm, a microtubule basket caught the nucleus, which thereafter was transformed elliptically. Microtubules were also observed along the elongated acrosome and mitochondrial derivatives. During apyrene spermiogenesis, however, the basal body was not attached to the nucleus and approached the head cyst cell after the completion of unidirectional arrangement, leaving the round nucleus in the middle of the cell. The presence or absence of the phenomenon in which the basal body attaches to the nucleus seems to be essential in the course of diverse spermatogenesis of the silkworm.     

Control of the eupyrene-apyrene sperm dimorphism in Lepidoptera

Lepidoptera males bear concomitantly nucleate (eupyrene) and anucleate (apyrene) spermatozoa. Both kinds of spermatozoa reach the spermatheca of inseminated females but only the eupyrene ones fertilize the eggs. The functions of the apyrene spermatozoa are still uncertain. Eupyrene spermatogenesis is regular and highly sensitive to genetic and experimental manipulations while apyrene spermatogenesis is irregular and withstands these manipulations. Both kinds of spermatozoa derive from the same kind of bipotential spermatocytes. The shift of spermatocyte commitment from eupyrene to apyrene spermatogenesis is induced by a haemolymph factor that becomes active just before or after pupation, depending on species. Accordingly, eupyrene spermatogenesis starts during larval instars and stops after pupation while apyrene spermatogenesis begins just before or after pupation, depending on the species, and persists in the imago. The shift is related to shortening of meiotic prophases and blocking synthesis of a meiotic lysine-rich protein fraction in apyrene cells. From spermatogonia proliferation to early spermatocytes, spermatogenesis is a quasi-independent process. Afterwards, it becomes discontinuous and is punctuated by predetermined stations. Progress to a subsequent station is an 'all or none' phenomenon, regulated by cues linked to fluctuations of the main morphogenetic hormones titers. In absence of a particular cue, the cells stop advancing towards the next station and eventually degenerate.     

Control of spermatogenesis resumption in post-diapausing larvae of the codling moth

The lepidopteran primary spermatocytes produce first eupyrene (nucleated) and later apyrene (anucleated) spermatozoa. The shift to apyrene commitment of the spermatocytes is related to an apyrene-spermatogenesis-inducing factor (ASIF) becoming active towards pupation. During diapause, the primary spermatocytes lyse and spermatogenesis ceases. The renewal of the dichotomous spermatogenesis in the testes of post-diapausing, last-instar larvae of the codling moth was studied in vivo and in vitro. In vivo, the post-diapausing larvae resume the two types of spermatogenesis. Since ASIF activity is related to pupation, the earliest apyrene spermatids appear one day before pupation, as in non-diapausing larvae. In vitro, renewal of spermatogenesis occurs if 20-hydroxy-ecdysone is added to the medium, but only eupyrene spermatids occur since the testes are explanted before ASIF activity has started. These spermatids are unreduced and develop directly from primary spermatocytes which do not undergo meiotic divisions. Moreover, only flagella develop in these spermatids and the nuclei remain spherical. Post-diapause resumption of spermatogenesis is thus a complex process in which meiosis-blocking and meiosis-deblocking factors, ecdysteroids, and the ASIF play regulative roles.     

Peristaltic squeezing of sperm bundles at the late stage of spermatogenesis in the silkworm, Bombyx mori

Silkworm (Lepidoptera) males produce dimorphic sperm, nucleate eupyrene sperm, and anucleate apyrene sperm. The eupyrene sperm is the ordinary sperm fertilizing eggs, while the function of the apyrene sperm, which are about four times as numerous as the eupyrene sperm, is still uncertain. We found the peristaltic phenomenon at the very late stage of spermatogenesis. Peristalsis occurs in both eupyrene and apyrene sperm bundles. Through peristaltic action, cytoplasm of the eupyrene sperm and both cytoplasm and nuclei of the apyrene sperm are discarded from the posterior end of the sperm bundles. Peristaltic squeezing seems to be a process to eliminate the irregular nuclei of apyrene sperm while preserving the nuclei of eupyrene sperm.     

Spermatogenesis in the testes of diapause and non-diapause pupae of the sweet potato hornworm, Agrius convolvuli (L.) (Lepidoptera: Sphingidae)

Dichotomous spermatogenesis was examined in relation to diapause in the sweet potato hornworm, Agrius convolvuli. In non-diapause individuals, eupyrene metaphase began during the fifth larval instar and eupyrene spermatids appeared in wandering larvae. Bundles of mature sperm were found after pupation. Apyrene spermatocytes also appeared during the fifth larval instar, but meiotic divisions occurred irregularly and their nuclei were discarded from the cells during spermiogenesis. Morphometric analyses of flagellar axonemes showed a variable sperm number in apyrene bundles. The variation ranging from 125 to 256 sperm per bundle indicated abnormal divisions or the elimination of apyrene spermatocytes. In diapause-induced hornworms, spermatogenesis progressed similarly during the larval stages. The cessation of spermatogenesis during diapause is characterized by 1) secondary spermatocytes and sperm bundles degenerating gradually as the diapause period lengthens, and 2) spermatogonia or primary spermatocytes appearing throughout diapause. A TUNEL (TdT-mediated dUTP-biotin nick end-labeling) assay revealed that DNA fragmentation occurred in the nuclei of secondary spermatocytes and early spermatids. Aggregates of heterochromatin along the nuclear membrane indicated the onset of apoptosis, and condensed chromatin was confirmed by electron microscopy to be the apoptotic body. These results show that the degenerative changes in spermatogenic cells during pupal diapause were controlled by apoptosis.     

BmPMFBP1 regulates the development of eupyrene sperm in the silkworm,Bombyx mori

Sperm deliver the male complement of DNA to the ovum, and thus play a key role in sexual reproduction. Accordingly, spermatogenesis has outstanding significance in fields as disparate as infertility treatments and pest-control, making it a broadly interesting and important focus for molecular genetics research in a wide range of species. Here we investigate spermatogenesis in the model lepidopteran insect Bombyx mori (silkworm moth), with particular focus on the gene PMFBP1 (polyamine modulated factor 1 binding protein 1). In humans and mouse, PMFBP1 is essential for spermatogenesis, and mutations of this gene are associated with acephalic spermatozoa, which cause infertility. We identified a B. mori gene labeled as “PMFBP1” in GenBank’s RefSeq database and sought to assess its role in spermatogenesis. Like in mammals, the silkworm version of this gene (BmPMFBP1) is specifically expressed in testes. We subsequently generated BmPMFBP1 mutants using a transgenic CRISPR/Cas9 system. Mutant males were sterile while the fertility of mutant females was comparable to wildtype females. In B. mori, spermatogenesis yields two types of sperm, the nucleated fertile eupyrene sperm, and anucleated unfertile apyrene sperm. Mutant males produced abnormal eupyrene sperm bundles but normal apyrene sperm bundles. For eupyrene sperm, nuclei were mislocated and disordered inside the bundles. We also found the BmPMFBP1 deficiency blocked the release of eupyrene sperm bundles from testes to ejaculatory seminalis. We found no obvious abnormalities in the production of apyrene sperm in mutant males, and double-matings with apyrene-deficient sex-lethal mutants rescued the ΔBmPMFBP1 infertility phenotype. These results indicate BmPMFBP1 functions only in eupyrene spermatogenesis, and highlight that distinct genes underlie the development of the two sperm morphs commonly found in Lepidoptera. Bioinformatic analyses suggest PMFBP1 may have evolved independently in lepidoptera and mammals, and that despite the shared name, are likely not homologous genes.     

Behavior of mitochondria during eupyrene and apyrene spermatogenesis in the silkworm,Bombyx mori (Lepidoptera), investigated by fluorescence in situ hybridization and electron microscopy

Summary Changes in the morphology and quantity of mitochondria and mitochondrial DNA during eupyrene and apyrene spermatogenesis in the silkworm were examined by electron microscopy and by fluorescence in situ hybridization with a 2 kb silkworm mitochondrial DNA clone (pBmMtE2). In the eupyrene spermatogenesis, the spermatocytes at early prophase I contained only a small amount of cytoplasm and showed a rather faint signal. As the cells grew larger in the later prophase I, the signal grew stronger. In the eupyrene spermatids, an especially strong signal was evident in the nebenkerns, in which all the cell's mitochondria were aggregated, and the strong fluorescence was maintained in mitochondrial derivatives. On the other hand, the apyrene cells were markedly smaller throughout spermatogenesis, showing much fainter signals for mitochondrial DNA than the eupyrene. Electron microscopy disclosed considerable differences in the behavior of mitochondria between the apýrene and the eupyrene cells. The observed qualitative and/or quantitative differences in the mitochondria may have some physiological bearing on the spermatogenesis of the two types of sperm.Abbreviations FISH fluorescence in situ hybridization - FITC fluorescein isothiocyanate - kb kilo base pair - PI propidium iodide - PBS phosphate-buffered saline